Guest guest Posted April 27, 2003 Report Share Posted April 27, 2003 In a message dated 4/27/03 6:53:33 PM Eastern Daylight Time, jbsmom@... writes: > What types of vitamins/supplements/diets are your children on and have you > found that these things have helped your children? I have been reading and > reading and there is just so many different things to try that I don't know > where to start, what to try etc. Cod liver oil, Vitamin C, Magnesium and Zinc and Selenium (only twice a week) I've also taken off milk. Just try to write down when you start trying something new and make notes to yourself on comments people make (ST OT etc) don't tell anyone what you're doing unless you think there might be a reason for them to know. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2003 Report Share Posted April 27, 2003 > I am not sure if this topic is appropriate for this list and I am NOT trying to start a debate. I have found this group so support and fun so if these questions are inappropriate, someone please tell me > Nope, not inappropriate! No one around here will DARE tell you what is " best " , so there's no problem! LOL. > What types of vitamins/supplements/diets are your children on and have you found that these things have helped your children? I have been reading and reading and there is just so many different things to try that I don't know where to start, what to try etc. > I tried SuperNuThera from Kirkman's Lab, a blend of B-something and something else...I have no idea how it affected because I could never get it into him!!! We used DMG (dimethylglicene, available at any health food store) and that really sped up his speech progress, then after a year lost its effect. This was the BEST supplement we used with him; while it was effective it seemed to perform miracles on the kid. We used TMG (trimethylglycine, from Kirkman's), and it made him very hyper, so we didn'd use it for very long. We don't use any supplements now, just clonidine (now called Dixoret here in ONtario or maybe Canada) for his hyperactivity. It's better because it's FREE under our drug plan <grin>. It has a slight effect on his ability to sit still and attend, but not as much as I'd like. So that's our history of supplements! If I was to endorse one, it would definitely be the DMG. Jacquie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2003 Report Share Posted April 27, 2003 Oh - I forgot diet! We went gfcf. It's a long story, but the last chapter reads that casein is absolute poison to 's brain (and mine as well), but gluten seems to have no adverse effect. Short version: within days of no casein, begain talking in sentences! Whenever casein enters his system (like when his idiot home therapist gave him cheetos, or his idiot father took him out for ice cream), he seems to vanish behind a wall of stims and off-the-wall behaviour. When the casein leaves his system, so do the stims. So we are a strict casein-free household that still eats grains, and that works for us! Jacquie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2003 Report Share Posted April 27, 2003 Thanks Jacquie! I keep reading about DMG so now I will definitely have to try it!! Is it a liquid? I think has an addiction (lack of a better word) to milk. When upset he drinks it and settles down. I have read about the GFCF diet and also the enzymes. I was already to go Casein free and chickened out with him starting school 2 weeks ago. Thanks for sharing and I look forward to hearing from others Warm Regards & ASD 11/25/00 in Maine Re: Vitamin/supplement/Diets > I am not sure if this topic is appropriate for this list and I am NOT trying to start a debate. I have found this group so support and fun so if these questions are inappropriate, someone please tell me > Nope, not inappropriate! No one around here will DARE tell you what is " best " , so there's no problem! LOL. > What types of vitamins/supplements/diets are your children on and have you found that these things have helped your children? I have been reading and reading and there is just so many different things to try that I don't know where to start, what to try etc. > I tried SuperNuThera from Kirkman's Lab, a blend of B-something and something else...I have no idea how it affected because I could never get it into him!!! We used DMG (dimethylglicene, available at any health food store) and that really sped up his speech progress, then after a year lost its effect. This was the BEST supplement we used with him; while it was effective it seemed to perform miracles on the kid. We used TMG (trimethylglycine, from Kirkman's), and it made him very hyper, so we didn'd use it for very long. We don't use any supplements now, just clonidine (now called Dixoret here in ONtario or maybe Canada) for his hyperactivity. It's better because it's FREE under our drug plan <grin>. It has a slight effect on his ability to sit still and attend, but not as much as I'd like. So that's our history of supplements! If I was to endorse one, it would definitely be the DMG. Jacquie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 28, 2003 Report Share Posted April 28, 2003 Hi , I have no problem answering the question and I'm curious to see what other people answer. If you want to ask me more questions about anything I'm doing, please contact me offlist or in IM, I'm more than happy to discuss it further. Jordan is Gluten-Free, Casein-Free. I haven't bothered to eliminate all the other stuff that you hear from other people (corn, soy, yadda yadda). He doesn't seem to have huge reactions to those things. Though I do try to limit the amount of soy he gets just because of health concerns with soy. Can't say I'm totally successful right now at limiting soy because he's not eating anything but crackers (soy meal ones right now, waiting for others to be in stock) and soy protein supplement in his rice milk. He gets Kirkman's ProBio Gold, a probiotic (the good gut flora) because he has intermittent problems with yeasty diarrhea. I had discontinued it but his DAN! Doctor told me to start it back up. His DAN! Doctor also just added cod liver oil (lemon flavored, imagine that) and I haven't been so good about making sure he gets that yet. Gotta really buckle down on it. I'm supposed to add a multivitamin called " Sea Silver " but I haven't found it in a healthfood store yet. The ultimate goal is to get him taking Super NuThera but he's unable to tolerate a lot of B-vitamins yet. I have enzymes to supplement his meals but he hasn't eaten table foods in over a month so he's not taking those right now. It sounds like a lot but really it's hardly anything compared to a lot of people I know. My ultimate goal is to get his gut healed so he doesn't *have* to take anything but a good multivitamin and maybe some enzymes with gluten or casein foods he eats occasionally. Debbie with twins - Jordan (ASD) 2.5yo - (NT) 2.5yo Quote Link to comment Share on other sites More sharing options...
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